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整合蛋白质组学和转录组学用于急性髓系白血病的系统性组合嵌合抗原受体疗法

Integrating Proteomics and Transcriptomics for Systematic Combinatorial Chimeric Antigen Receptor Therapy of AML.

作者信息

Perna Fabiana, Berman Samuel H, Soni Rajesh K, Mansilla-Soto Jorge, Eyquem Justin, Hamieh Mohamad, Hendrickson Ronald C, Brennan Cameron W, Sadelain Michel

机构信息

Center for Cell Engineering and Immunology Program, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Microchemistry and Proteomics Core Laboratory, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

出版信息

Cancer Cell. 2017 Oct 9;32(4):506-519.e5. doi: 10.1016/j.ccell.2017.09.004.

Abstract

Chimeric antigen receptor (CAR) therapy targeting CD19 has yielded remarkable outcomes in patients with acute lymphoblastic leukemia. To identify potential CAR targets in acute myeloid leukemia (AML), we probed the AML surfaceome for overexpressed molecules with tolerable systemic expression. We integrated large transcriptomics and proteomics datasets from malignant and normal tissues, and developed an algorithm to identify potential targets expressed in leukemia stem cells, but not in normal CD34CD38 hematopoietic cells, T cells, or vital tissues. As these investigations did not uncover candidate targets with a profile as favorable as CD19, we developed a generalizable combinatorial targeting strategy fulfilling stringent efficacy and safety criteria. Our findings indicate that several target pairings hold great promise for CAR therapy of AML.

摘要

靶向CD19的嵌合抗原受体(CAR)疗法在急性淋巴细胞白血病患者中取得了显著疗效。为了确定急性髓系白血病(AML)中潜在的CAR靶点,我们在AML表面组中探寻具有可耐受全身表达的过表达分子。我们整合了来自恶性和正常组织的大型转录组学和蛋白质组学数据集,并开发了一种算法,以识别在白血病干细胞中表达,但在正常CD34CD38造血细胞、T细胞或重要组织中不表达的潜在靶点。由于这些研究未发现具有与CD19一样有利特征的候选靶点,我们制定了一种满足严格疗效和安全性标准的通用组合靶向策略。我们的研究结果表明,几种靶点配对在AML的CAR治疗中具有很大的前景。

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